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FDA 510(k)

OPERATING ROOM TOWELS -STERILE & NON-STERILE

K-Number: K881396 · 1988-04-29

ApplicantA Plus International, Inc.
Decision Date1988-04-29
Product CodeKKX
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

OPERATING ROOM TOWELS -STERILE & NON-STERILE is the device name listed in this FDA 510(k) record. The listed applicant is A Plus International, Inc.. It received FDA 510(k) clearance on 1988-04-29 under 510(k) number K881396. The device is classified under product code KKX. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the OPERATING ROOM TOWELS -STERILE & NON-STERILE?

OPERATING ROOM TOWELS -STERILE & NON-STERILE is a medical device that received FDA 510(k) clearance on 1988-04-29. The listed applicant is A Plus International, Inc.. The 510(k) number is K881396.

When did OPERATING ROOM TOWELS -STERILE & NON-STERILE receive FDA 510(k) clearance?

OPERATING ROOM TOWELS -STERILE & NON-STERILE received FDA 510(k) clearance on 1988-04-29, under 510(k) number K881396.

Who is the listed applicant for OPERATING ROOM TOWELS -STERILE & NON-STERILE?

The FDA 510(k) record lists A Plus International, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for OPERATING ROOM TOWELS -STERILE & NON-STERILE?

The FDA product code for OPERATING ROOM TOWELS -STERILE & NON-STERILE is KKX.

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Other records listing A Plus International, Inc. as applicant

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K213001Procedure Mask, Surgical MaskK102861SURGIPLUS SMS SURGICAL DRAPE (STERILE/NON-STERILE), SURGIPLUS SPP WITH PE LAMINATED SURGICAL DRAPE (STERILE/NON-STERILE)K093169SURGIPLUS STANDARD SURGICAL GOWN (STERILE) ( NON STERILE), REINFORCED SURGICAL GOWN (STERILE) (NON STERILE)K031353SOLUTION FACE MASKSK882284SURGEONS CAPK882283BOUFFANT CAP

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Related Devices (Code: KKX)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K230645BeneHold™ Surgical Incise Drape with CHG antimicrobial IIAvery Dennison Medical , Ltd.K2225783M™ Ioban™ CHG Chlorhexidine Gluconate Incise Drape (contains 2% w/w CHG)3M CompanyK202208BeneHold Surgical Incise Drape with CHG antimicrobialAvery Dennison Belgie BvbaK200238ControlRad Sterile CoverControlrad, Inc.K163556MediClear PreOpCovalontechnologies, Inc.K130404TIBURON SURGICAL DRAPECardinal Health200, LLC

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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